FDA Inspection 1067650 — ImpactLife

ImpactLife — FEI 1470254

The FDA completed an inspection of ImpactLife on Sep 13, 2018 in Springfield, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 13, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Springfield, IL (United States)